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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Water-Electrolyte Imbalance (D014883)
..Starting node ..Hyperkalemia (D006947)
Child Nodes:
........Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly (C563840)
........Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema (C566369)
........Pseudohyperkalemia Cardiff (C535827)
........Pseudohyperkalemia, Familial, 2, due to Red Cell Leak (C563785)
Sister Nodes:
..Dehydration (D003681)
..Hypercalcemia (D006934) 10
..Hyperkalemia (D006947) 4
..Hypernatremia (D006955)
..Hypocalcemia (D006996) 5
..Hypokalemia (D007008) 1
..Hyponatremia (D007010) 1
..Inappropriate ADH Syndrome (D007177) 1
..Water Intoxication (D014869)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5397
Name:	Hyperkalemia
Definition:	Abnormally high potassium concentration in the blood, most often due to defective renal excretion. It is characterized clinically by electrocardiographic abnormalities (elevated T waves and depressed P waves, and eventually by atrial asystole). In severe cases, weakness and flaccid paralysis may occur. (Dorland, 27th ed)
Alternative IDs:
ParentIDs:	MESH:D014883
TreeNumbers:	C18.452.950.396
Synonyms:	Hyperkalemias \|Hyperpotassemia \|Hyperpotassemias
Slim Mappings:	Metabolic disease
Reference:	MedGen: D006947 MeSH: D006947 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants